Canonical Allele Identifier: CA1839056695
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756006C= , CM000671.2:g.21756006C= GRCh38
NC_000009.11:g.21756005C= , CM000671.1:g.21756005C= GRCh37
NC_000009.10:g.21746005C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746563.2:n.163+11819G=